Label: DR.S CLEAN ADVANCED HAND SANITIZER- ethyl alcohol gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 55526-0017-1 - Packager: EQMAXON Corp.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 29, 2021
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENTS
- PURPOSE
-
WARNINGS
Flammable. Keep away from fire and flames. For external use only.
When using this product • Do not get into eyes. • If contact occurs, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or redness develops.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- Questions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DR.S CLEAN ADVANCED HAND SANITIZER
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55526-0017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 700 mL in 1000 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) ALOE (UNII: V5VD430YW9) Glycerin (UNII: PDC6A3C0OX) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) Butylene Glycol (UNII: 3XUS85K0RA) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55526-0017-1 1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 06/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/01/2021 Labeler - EQMAXON Corp. (557821534) Registrant - EQMAXON Corp. (557821534) Establishment Name Address ID/FEI Business Operations EQMAXON Corp. 557821534 manufacture(55526-0017)